Intractable Epilepsy and Progressive Cognitive Decline in a Young Man
JAMA Neurol 74:737-740, Cohen, A.L.,et al, 2017
Huntington Disease: Clinical Features and Diagnosis
UptoDate Dec 2017, Oksana Suchowersky, 2017
Non-Alzheimers Dementia 1 Frontotemporal Dementia
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Genetic Aspects of Alzheimer Disease
The Neurologist 15:80-86, Williamson,J.,et al, 2009
The Genetics of Alzheimer Disease, Current Status and Future Prospects
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Hereditary Form of Parkinsonism-Dementia
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Clinicopath Conf
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Clinicopath Conf
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Predisposing Locus for Alzheimer's Disease on Chromosome 21
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Niemann-Pick Type C Disease
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A 60-Year-Old Man with Weakness and Gait Dysfunction
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Neonatal Seizures
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Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease
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The Phenotypic Continuum of ATP1A3-Related Disorders
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Personality Changes, Executive Dysfunction, and Motor and Memory Impairment
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Molybdenum Cofactor Deficiency
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Sturge-Weber Syndrome
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Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder
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Clinicopath Conf., Adult Cerebral Form of X-Linked Adrenoleukodystrophy
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Parkinsons Disease and Genetics
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Epilepsy Syndromes in Infancy
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Clinical Spectrum of Succinic Semialdehyde Dehydrogenase Deficiency
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Fragile X Premutation Carriers: Characteristic MR Imaging Findings of Adult Male Patients with Progressive Cerebellar and Cognitive Dysfunction.
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Adult-Onset Leukoencephalopathy with Vanishing White Matter Presenting with Dementia
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Association Between Early-Onset Parkinson's Disease and Mutations in the Parkin Gene
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Genetic Studies on Chromosome 12 in Late-Onset Alzheimer Disease
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Familial Aggregation in Frontotemporal Dementia
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The Clinical Introduction of Genetic Testing for Alzheimer Disease, An Ethical Perspective
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X Linked Adrenoleukodystrophy:Clinical Presentation, Diagnosis, and Therapy
JNNP 63:4-14, vanGeel,B.M.,et al, 1997
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A Large Kindred with Autosomal Dominant Parkinson's Disease
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